Asia-Pacific Uveitis Therapeutics Markets to 2023 - Market will be Valued at $405.5m

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Mar 15, 2018, 02:30 ET

DUBLIN, March 15, 2018 /PRNewswire/ --

The "Uveitis Therapeutics in Asia-Pacific Markets to 2023 - Increasing Prevalence, Continued Uptake of Biologics and Novel Pipeline Drugs to Drive the Market" report has been added to ResearchAndMarkets.com's offering.

The Asia-Pacific uveitis market will be valued at $405.5m in 2023, growing from $179m in 2016, at a compound annual growth rate of 12.4%.

It is a leading cause of blindness in both developed and developing countries and is the fifth most common cause of vision loss in the developed world. The uveitis market is characterized by a small selection of marketed drug options, consisting of corticosteroid therapies, immunosuppressive therapies and biologics. Historically, corticosteroid therapies have made up the bulk of the uveitis market.

Currently only one targeted therapy is available in the Asia-Pacific uveitis market, which is AbbVie's Humira (adalimumab). The late-stage uveitis pipeline is composed of Santen's Opsiria and Clearside Biomedical's CLS-TA, which are expected to be highly lucrative and address some of the unmet needs.

These new drugs will expand the options available to treat uveitis patients and contribute to overall market growth by offering novel treatment mechanisms, including new drug delivery routes and novel, non-corticosteroid drug molecules.

Scope

What are the key factors driving the Asia-Pacific uveitis treatment market?
How will targeted therapies such as Humira contribute to growth?
Do branded therapies show continuous growth, and are they facing competition from generics?
How will branded therapies be affected by upcoming pipeline therapies?
Corticosteroid therapies dominate the uveitis market, but unmet needs exist in terms of safety and efficacy. Will the drugs under development fulfill the unmet needs?
What are the common targets and mechanisms of action of pipeline therapies?
What are the commercial prospects for the most promising late-stage products?
Various drivers and barriers will influence the market over the forecast period.
What are the barriers that will limit the uptake of premium-priced therapies in the assessed countries?
Which factors are most likely to drive the market in these countries?
What licensing and co-development deals have occurred within this therapy area since 2006?

Key Topics Covered:

1 Table of Contents

2 Introduction
2.1 Disease Introduction
2.2 Epidemiology
2.3 Symptoms
2.4 Etiology and Pathophysiology
2.4.1 Autoimmune uveitis
2.4.2 Non-autoimmune uveitis
2.5 Diagnosis
2.6 Prognosis
2.7 Treatment Options
2.7.1 Corticosteroids
2.7.2 Immunosuppressive Agents
2.7.3 Biologics
2.7.4 Adjuvant Therapy

3 Marketed Products
3.1 Overview
3.1.1 Humira (adalimumab) - AbbVie
3.1.2 Retisert (fluocinolone acetonide) - Bausch & Lomb
3.1.3 Ozurdex (dexamethasone) - Allergan
3.1.4 Neoral (Cyclosporine) - Novartis
3.1.5 Mycept (Mycophenolate mofetil) - Panacea Biotec
3.1.6 Medrol (Methylprednisolone) - Pfizer
3.1.7 Betamethasone - Merck & Co.
3.1.8 Pred Forte (Prednisolone) - Allergan
3.2 Comparative Efficacy and Safety of Marketed Products

4 Pipeline Analysis
4.1 Overview
4.2 Pipeline by Stage of Development, Molecule Type, Route of Administration and Program Type
4.3 Pipeline by Molecular Target
4.4 Promising Pipeline Candidates
4.4.1 DE-109/ Opsiria (Sirolimus) - Santen
4.4.2 CLS-TA (triamcinolone acetonide) - Clearside BioMedical
4.5 Heatmap for Pipeline Products
4.6 Product Competitiveness Framework

5 Clinical Trial Analysis
5.1 Failure Rate
5.1.1 Overall Failure Rate
5.1.2 Failure Rate by Phase and Molecule Type
5.1.3 Failure Rate by Phase and Molecular Target
5.2 Clinical Trial Size
5.2.1 Patient Enrollment per Product by Molecule Type and Stage of Development
5.2.2 Patient Enrollment per Product by Molecular Target and Stage of Development
5.2.3 Patient Enrollment per Trial by Molecule Type and Stage of Development
5.2.4 Patient Enrollment per Trial by Molecular Target and Stage of Development
5.3 Clinical Trial Duration
5.3.1 Trial Duration by Molecule Type and Stage of Development
5.3.2 Trial Duration by Molecular Target and Stage of Development
5.4 Summary of Clinical Trial Metrics

6 Multi-scenario Forecast
6.1 Geographical Markets
6.2 Asia-Pacific Market
6.3 India
6.4 China
6.5 Australia
6.6 South Korea
6.7 Japan

7 Drivers and Barriers
7.1 Drivers
7.1.1 Increasing Usage of Biologics
7.1.2 Promising Late-Stage Pipeline Products Can Change Treatment Paradigm
7.1.3 Increasing Elderly Population and Incidence of Uveitis
7.2 Barriers
7.2.1 Uveitis - An Under-Researched Disease
7.2.2 Low Diagnosis and Treatment Rates
7.2.3 Steep Prices of Therapeutics to Slow Down Market Growth

8 Deals and Strategic Consolidations
8.1 Licensing Deals
8.1.1 Deals by Region and Value
8.1.2 Number of Disclosed and Undisclosed Deals by Year, Aggregate Deal Value
8.1.3 Deal Value by Stage of Development, Molecule Type, and Molecular Target
8.1.4 Key Licensing Deals
8.2 Co-development Deals
8.2.1 Deals by region, value, year, stage of development, molecule type and molecular target
8.2.2 Key Co-development Deals

9 Appendix
9.1 All Pipeline Drugs by Stage of Development
9.1.1 Discovery
9.1.2 Preclinical
9.1.3 IND/CTA-filed
9.1.4 Phase I
9.1.5 Phase II
9.1.6 Phase III
9.1.7 Pre-registration
9.2 Market Forecasts to 2023
9.2.1 Asia-Pacific
9.2.2 India
9.2.3 China
9.2.4 Australia
9.2.5 South Korea
9.2.6 Japan
9.3 Bibliography
9.4 Abbreviations
9.5 Research Methodology
9.5.1 Secondary Research
9.5.2 Marketed Product Profiles
9.5.3 Late-Stage Pipeline Candidates
9.5.4 Comparative Efficacy and Safety Heatmap for Marketed and Pipeline Products
9.5.5 Product Competitiveness Framework
9.5.6 Pipeline Analysis
9.5.7 Forecasting Model
9.5.8 Deals Data Analysis
9.6 Contact
9.7 Disclaimer

For more information about this report visit https://www.researchandmarkets.com/research/cjxfh2/_asiapacific?w=5

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